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Items: 1 to 20 of 71

1.

Perioperative genomic profiles using structure-specific oligonucleotide probes.

Hogan KJ, Burmester JK, Caldwell MD, Hogan QH, Coursin DB, Green DN, Selzer RM, Broderick TP, Rusy DA, Poroli M, Lutz AL, Sanders AM, Oldenburg MC, Koelbl JA, de Arruda-Indig M, Halsey JL, Day SP, Domanico MJ.

Clin Med Res. 2009 Sep;7(3):69-84. doi: 10.3121/cmr.2009.837. Epub 2009 May 27.

2.

Association between two unlinked loci at 8q24 and prostate cancer risk among European Americans.

Zheng SL, Sun J, Cheng Y, Li G, Hsu FC, Zhu Y, Chang BL, Liu W, Kim JW, Turner AR, Gielzak M, Yan G, Isaacs SD, Wiley KE, Sauvageot J, Chen HS, Gurganus R, Mangold LA, Trock BJ, Gronberg H, Duggan D, Carpten JD, Partin AW, Walsh PC, Xu J, Isaacs WB.

J Natl Cancer Inst. 2007 Oct 17;99(20):1525-33. Epub 2007 Oct 9.

PMID:
17925536
3.

5 HT(3)-receptor antagonists and cardiac repolarization time in patients expressing a novel genetic target associated with baseline QTc interval abnormalities.

Quraishi SA, Schuler GH, Janicki PK.

J Clin Anesth. 2011 Jun;23(4):297-302. doi: 10.1016/j.jclinane.2010.11.003.

PMID:
21663814
4.

Thiopurine methyltransferase gene polymorphisms in Chinese patients with inflammatory bowel disease.

Cao Q, Zhu Q, Shang Y, Gao M, Si J.

Digestion. 2009;79(1):58-63. doi: 10.1159/000205268. Epub 2009 Feb 28.

PMID:
19252404
5.

Genetic variation analysis in parkinson disease patients with and without hallucinations: case-control study.

Goetz CG, Burke PF, Leurgans S, Berry-Kravis E, Blasucci LM, Raman R, Zhou L.

Arch Neurol. 2001 Feb;58(2):209-13.

PMID:
11176958
6.

Mutant genes of cytochrome P-450IID6, glutathione S-transferase class Mu, and arylamine N-acetyltransferase in lung cancer patients.

Roots I, Brockmöller J, Drakoulis N, Loddenkemper R.

Clin Investig. 1992 Mar-Apr;70(3-4):307-19.

PMID:
1355678
7.

Exploring the genetic role of the HLA-DPB1 locus in Chileans with intrahepatic cholestasis of pregnancy.

Mella JG, Roschmann E, Glasinovic JC, Alvarado A, Scrivanti M, Volk BA.

J Hepatol. 1996 Mar;24(3):320-3.

PMID:
8778199
8.

Detection of His1069Gln mutation in Wilson disease by bidirectional PCR amplification of specific alleles (BI-PASA) test.

Poláková H, Katrincsáková B, Minárik G, Feráková E, Ficek A, Baldovic M, Kádasi L.

Gen Physiol Biophys. 2007 Jun;26(2):91-6.

PMID:
17660582
9.

Effect of the CYP2D6*10 C188T polymorphism on postoperative tramadol analgesia in a Chinese population.

Wang G, Zhang H, He F, Fang X.

Eur J Clin Pharmacol. 2006 Nov;62(11):927-31. Epub 2006 Sep 8.

PMID:
16960721
10.

BCHE and CYP2D6 genetic variation in Alzheimer's disease patients treated with cholinesterase inhibitors.

Chianella C, Gragnaniello D, Maisano Delser P, Visentini MF, Sette E, Tola MR, Barbujani G, Fuselli S.

Eur J Clin Pharmacol. 2011 Nov;67(11):1147-57. doi: 10.1007/s00228-011-1064-x. Epub 2011 Jun 1.

PMID:
21630031
11.

Rationale and study design of the CardioGene Study: genomics of in-stent restenosis.

Ganesh SK, Skelding KA, Mehta L, O'Neill K, Joo J, Zheng G, Goldstein J, Simari R, Billings E, Geller NL, Holmes D, O'Neill WW, Nabel EG.

Pharmacogenomics. 2004 Oct;5(7):952-1004.

PMID:
15469413
12.
13.

The pharmacogenetics of immunosuppression for organ transplantation: a route to individualization of drug administration.

Fredericks S, Holt DW, MacPhee IA.

Am J Pharmacogenomics. 2003;3(5):291-301. Review.

PMID:
14575518
14.

Genotypic analysis of thiopurine S-methyltransferase in patients with Crohn's disease and severe myelosuppression during azathioprine therapy.

Colombel JF, Ferrari N, Debuysere H, Marteau P, Gendre JP, Bonaz B, Soulé JC, Modigliani R, Touze Y, Catala P, Libersa C, Broly F.

Gastroenterology. 2000 Jun;118(6):1025-30.

PMID:
10833476
15.

Genetic heterogeneity in familial dysbetalipoproteinemia. The E2(lys146----gln) variant results in a dominant mode of inheritance.

Smit M, de Knijff P, van der Kooij-Meijs E, Groenendijk C, van den Maagdenberg AM, Gevers Leuven JA, Stalenhoef AF, Stuyt PM, Frants RR, Havekes LM.

J Lipid Res. 1990 Jan;31(1):45-53.

16.

AN EPIDEMIOLOGICAL STUDY OF THIOPURINE-METHYLTRANSFERASE VARIANTS IN A CROATIAN INFLAMMATORY BOWEL DISEASE PATIENT COHORT.

Ladić A, Božina N, Borzan V, Brinar M, Vucelić B, Cuković-Cavka S.

Acta Clin Croat. 2016 Mar;55(1):16-22.

PMID:
27333713
17.

Angiotensin-converting enzyme gene polymorphism may influence blood loss in a geriatric population undergoing total hip arthroplasty.

Pola E, Gaetani E, Pola R, Papaleo P, Flex A, Aloi F, De Santis V, Santoliquido A, Pola P.

J Am Geriatr Soc. 2002 Dec;50(12):2025-8.

PMID:
12473016
18.

Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation.

Mein CA, Barratt BJ, Dunn MG, Siegmund T, Smith AN, Esposito L, Nutland S, Stevens HE, Wilson AJ, Phillips MS, Jarvis N, Law S, de Arruda M, Todd JA.

Genome Res. 2000 Mar;10(3):330-43.

19.

The CYP3A4*1B allele increases risk for small cell lung cancer: effect of gender and smoking dose.

Dally H, Edler L, Jäger B, Schmezer P, Spiegelhalder B, Dienemann H, Drings P, Schulz V, Kayser K, Bartsch H, Risch A.

Pharmacogenetics. 2003 Oct;13(10):607-18.

PMID:
14515059
20.

Pharmacogenomics as molecular autopsy for forensic toxicology: genotyping cytochrome P450 3A4*1B and 3A5*3 for 25 fentanyl cases.

Jin M, Gock SB, Jannetto PJ, Jentzen JM, Wong SH.

J Anal Toxicol. 2005 Oct;29(7):590-8.

PMID:
16419387

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